catalog number :
MBS534654
products full name :
VWF antibody (HRP)
products short name :
VWF
products name syn :
Polyclonal VWF; Anti-VWF; Von Willebrand Factor
other names :
von Willebrand factor; von Willebrand factor; von Willebrand factor; von Willebrand factor; von Willebrand antigen 2Alternative name(s):von Willebrand antigen II
other gene names :
VWF; VWF; VWD; F8VWF; F8VWF; vWF
uniprot entry name :
VWF_HUMAN
form :
Supplied in liquid form with 10 mM HEPES, pH 7.4, 150 mM NaCl, 50% (v/v) glycerol.
storage stability :
Store at -10 to -20 degree C. Product will become viscous but will not freeze. Avoid storage in frost-free freezers. Allow product to warm to room temperature and gently mix before use.
tested application :
User optimized
other info1 :
Biological Significance: Von Willebrand factor (vWF) is a blood glycoprotein involved in hemostasis. It is deficient or defective in von Willebrand disease and is involved in a large number of other diseases, including thrombotic thrombocytopenic purpura, Heyde's syndrome, and possibly hemolytic-uremic syndrome.
other info2 :
Tag/Conjugate: HRP. Immunogen: VWF antibody (HRP) was raised in goat using human vWF purified from plasma as the immunogen.
products categories :
Cell Biology; Conjugated Polyclonal Antibodies
products description :
Goat polyclonal VWF antibody (HRP) conjugated
ncbi acc num :
AAB59458.1
ncbi mol weight :
38,745 Da
ncbi pathways :
Blood Clotting Cascade Pathway 198840!!Complement And Coagulation Cascades Pathway 198880!!Complement And Coagulation Cascades Pathway 83073!!Complement And Coagulation Cascades Pathway 484!!ECM-receptor Interaction Pathway 83068!!ECM-receptor Interaction Pathway 479!!Focal Adhesion Pathway 198795!!Focal Adhesion Pathway 83067!!Focal Adhesion Pathway 478!!Formation Of Fibrin Clot (Clotting Cascade) Pathway 106057
ncbi summary :
The glycoprotein encoded by this gene functions as both an antihemophilic factor carrier and a platelet-vessel wall mediator in the blood coagulation system. It is crucial to the hemostasis process. Mutations in this gene or deficiencies in this protein result in von Willebrand's disease. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Jul 2008]